Canonical Allele Identifier: CA2245346701
Gene: AIPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425563G= , CM000679.2:g.6425563G= GRCh38
NC_000017.10:g.6328883G= , CM000679.1:g.6328883G= GRCh37
NC_000017.9:g.6269607G= NCBI36
NG_008474.1:g.14637C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.1052C= MANE Select ENSP00000370521.3:p.Pro351=
ENST00000250087.9:c.863C= ENSP00000250087.5:p.Pro288=
ENST00000381128.2:c.*924C= ENSP00000370520.2:n.*924C=
ENST00000381129.7:c.1052C= ENSP00000370521.3:p.Pro351=
ENST00000570466.5:c.986C= ENSP00000461287.1:p.Pro329=
ENST00000570584.5:c.251+8356C=
ENST00000574506.5:c.1016C= ENSP00000458456.1:p.Pro339=
ENST00000575265.5:c.*1023C= ENSP00000459673.1:n.*1023C=
ENST00000576307.5:c.872C= ENSP00000459522.1:p.Pro291=
ENST00000576776.5:c.980C= ENSP00000460827.1:p.Pro327=
ENST00000621374.4:c.*70C= ENSP00000481337.1:n.*70C=
NM_001033054.2:c.863C= NP_001028226.1:p.Pro288=
NM_001033055.2:c.872C= NP_001028227.1:p.Pro291=
NM_001285399.2:c.1016C= NP_001272328.1:p.Pro339=
NM_001285400.2:c.986C= NP_001272329.1:p.Pro329=
NM_001285401.2:c.980C= NP_001272330.1:p.Pro327=
NM_001285402.1:c.935C= NP_001272331.1:p.Pro312=
NM_014336.4:c.1052C= NP_055151.3:p.Pro351=
NM_001033054.3:c.863C= NP_001028226.1:p.Pro288=
NM_001033055.3:c.872C= NP_001028227.1:p.Pro291=
NM_001285399.3:c.1016C= NP_001272328.1:p.Pro339=
NM_001285400.3:c.986C= NP_001272329.1:p.Pro329=
NM_001285401.3:c.980C= NP_001272330.1:p.Pro327=
NM_001285402.2:c.935C= NP_001272331.1:p.Pro312=
NM_001285403.3:c.*1023C= NP_001272332.1:n.*1023C=
NM_014336.5:c.1052C= MANE Select NP_055151.3:p.Pro351=
NM_001285403.4:c.*1023C= NP_001272332.1:n.*1023C=